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ACAAAGATTTAGGGGGCTTATGAAG[C/G]TCACCATGAGCAGCTCCCACTAATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610666 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101929937 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LOC101929937 - uncharacterized LOC101929937 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017028182.1 | Intron | XP_016883671.1 |
NRSN2 - neurensin 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323679.1 | Intron | NP_001310608.1 | ||||
NM_001323680.1 | Intron | NP_001310609.1 | ||||
NM_001323681.1 | Intron | NP_001310610.1 | ||||
NM_001323682.1 | Intron | NP_001310611.1 | ||||
NM_001323683.1 | Intron | NP_001310612.1 | ||||
NM_001323684.1 | Intron | NP_001310613.1 | ||||
NM_001323685.1 | Intron | NP_001310614.1 | ||||
NM_024958.2 | Intron | NP_079234.1 | ||||
XM_006723630.3 | Intron | XP_006723693.1 | ||||
XM_011529360.1 | Intron | XP_011527662.1 | ||||
XM_011529362.2 | Intron | XP_011527664.1 | ||||
XM_011529363.2 | Intron | XP_011527665.1 | ||||
XM_017028073.1 | Intron | XP_016883562.1 | ||||
XM_017028074.1 | Intron | XP_016883563.1 | ||||
XM_017028075.1 | Intron | XP_016883564.1 | ||||
XM_017028076.1 | Intron | XP_016883565.1 |